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PMCF-study Using Novosyn® Quick Suture Material for Perineal Repair After Episiotomy — EPINOQ  

Episiotomy Clinical Trial

Official title:
Post-Marketing Clinical Follow-up (PMCF) Study to Evaluate the Safety and Efficacy of Novosyn® Quick Suture Material for Episiotomy . A Monocenter, Prospective, Observational Study.

Clinical Trial Summary

The aim of this study is to show that the performance of Novosyn® Quick suture material is comparable with other suture material used for episiotomy. In order to show that, various safety and efficacy parameters have been selected. The outcome regarding these parameters will be evaluated by a quantitative summary of the available clinical data from the literature. Study population consists of women with a spontaneous vaginal delivery who required perineal repair due to an episiotomy.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02762357
Study type Observational
Source Aesculap AG
Contact
Status Completed
Phase
Start date September 2016
Completion date January 7, 2020
View Details
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